8 results match your criteria: "Materials Science Research Institute (MSRI)[Affiliation]"
ACS Omega
December 2022
National Petrochemical Technology Center (NPTC), Materials Science Research Institute (MSRI), King Abdulaziz City for Science and Technology (KACST), P.O. Box 6086, Riyadh11442, Saudi Arabia.
The carbon dioxide reforming of methane has attracted attention from researchers owing to its possibility of both mitigating the hazards of reactants and producing useful chemical intermediates. In this framework, the activity of the nickel-based catalysts, supported by yttria-stabilized zirconia and promoted with holmium oxide (HoO), was assessed in carbon dioxide reforming of methane at 800 °C. The catalysts were characterized by N-physisorption, H temperature-programmed reduction, temperature-programmed desorption of CO, X-ray diffraction, scanning electron microscopy (SEM) together with energy-dispersive X-ray spectroscopy, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA) techniques.
View Article and Find Full Text PDFMaterials (Basel)
March 2022
Geobiotec Research Centre, Department of Geoscience, University of Aveiro, 3810-193 Aveiro, Portugal.
With rapid industrialization, there is an ever-increasing demand for iron oxides, calcium oxides, aluminum oxides, silica, and zeolites as raw materials for various industries, but reserves of such metal oxides are continuously diminishing. Therefore, there is an urgent need to explore new alternatives for such value-added minerals. One such material is incense stick ash (ISA), which is among the most unexplored byproducts from residential and holy places.
View Article and Find Full Text PDFNanomaterials (Basel)
October 2021
Institute for Quantum Science and Engineering, Texas A&M University, College Station, TX 77843, USA.
In this work, we report an easy, efficient method to synthesize high quality lithium-based upconversion nanoparticles (UCNPs) which combine two promising materials (UCNPs and lithium ions) known to enhance the photovoltaic performance of perovskite solar cells (PSCs). Incorporating the synthesized YLiF:Yb,Er nanoparticles into the mesoporous layer of the PSCs cells, at a certain doping level, demonstrated a higher power conversion efficiency (PCE) of 19%, additional photocurrent, and a better fill factor (FF) of 82% in comparison to undoped PSCs (PCE = ~16.5%; FF = 71%).
View Article and Find Full Text PDFSci Rep
August 2020
National Petrochemical Technology Center (NPTC), Materials Science Research Institute (MSRI), King Abdulaziz City for Science and Technology, P.O. Box 6086, Riyadh, 11442, Saudi Arabia.
The generation of synthesis gas (hydrogen and carbon monoxide mixture) from two global warming gases of carbon dioxide and methane via dry reforming is environmentally crucial and for the chemical industry as well. Herein, magnesium-promoted NiO supported on mesoporous zirconia, 5Ni/xMg-ZrO (x = 0, 3, 5, 7 wt%) were prepared by wet impregnation method and then were tested for syngas production via dry reforming of methane. The reaction temperature at 800 °C was found more catalytically active than that at 700 °C due to the endothermic feature of reaction which promotes efficient CH catalytic decomposition over Ni and Ni-Zr interface as confirmed by CH-TSPR experiment.
View Article and Find Full Text PDFHeliyon
January 2019
National Petrochemical Technology Center (NPTC), Materials Science Research Institute (MSRI), King Abdulaziz City for Science and Technology (KACST), PO Box 6086, Riyadh, 11442, Saudi Arabia.
We successfully synthesized 3D supramolecular structure of cyclohexylammonium tetraisothiocyanatocobaltate(II) complex, (CHNH)[Co(NCS)], in almost a quantitative yield by using metathesis and ligand addition reactions. The new complex was characterized by various techniques such as FTIR, UV-Visible, PXRD, SXRD, and CV electrochemical analysis to investigate mainly its structure. Based on the results of these techniques, the formation of the desired complex was confirmed.
View Article and Find Full Text PDFSmall
February 2016
Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Molecular Engineering of Polymers, Laboratory of Advanced Materials, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai, 200433, China.
Well ordered, uniform 3D open macro/mesoporous TiO2 hollow microspheres with highly crystalline anatase thin shells have been successfully synthesized by a simple solvent evaporation-driven confined self-assembly method. The 3D open macro/mesoporous TiO2 hollow microspheres show high energy-conversion efficiency (up to 9.5%) and remarkable photocatalytic activity (with photodegradation of 100% for methylene blue in 12 min under UV light irradiation).
View Article and Find Full Text PDFSci Adv
May 2015
Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Key Laboratory of Molecular Engineering of Polymers, i ChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Laboratory of Advanced Materials, Fudan University, Shanghai 200433, China.
Highly crystalline mesoporous materials with oriented configurations are in demand for high-performance energy conversion devices. We report a simple evaporation-driven oriented assembly method to synthesize three-dimensional open mesoporous TiO2 microspheres with a diameter of ~800 nm, well-controlled radially oriented hexagonal mesochannels, and crystalline anatase walls. The mesoporous TiO2 spheres have a large accessible surface area (112 m(2)/g), a large pore volume (0.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
January 2015
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, PO Box 2457, Riaydh 11451, Saudi Arabia ; X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia.
In the title salt, C6H11NH3 (+)·SCN(-), the cyclo-hexyl-ammonium ring adopts a slightly distorted chair conformation. The ammonium group occupies an equatorial position to minimize 1,3 and 1,5 diaxial inter-actions. In the crystal, the components are linked by N-H⋯N and N-H⋯S hydrogen-bonding inter-actions, resulting in a three-dimensional network.
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